A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556917



Internal ID15997640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:757691..765362hg38UCSC Ensembl
Innerchr12:866857..874528hg19UCSC Ensembl
Innerchr12:737118..744789hg18UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg387672
hg197672
hg187672
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2259n54
Supporting Variantsnssv786069, nssv786068, nssv786073, nssv786065, nssv786072, nssv786070, nssv786067, nssv786066, nssv786071
Samples
Known GenesWNK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556917
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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